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  • 1990-1994  (2)
  • 1993  (2)
  • Contarinia sorghicola  (1)
  • Serotonin  (1)
  • 1
    Electronic Resource
    Electronic Resource
    p-Chlorophenylalanine, a serotonin synthesis inhibitor, reduces the response of glial fibrillary acidic protein induced by trauma to the spinal cord (1993)
    Springer
    Acta neuropathologica 86 (1993), S. 422-427 
    Details
    ISSN: 1432-0533
    Keywords: Spinal cord trauma ; Glial fibrillary acidic protein ; Serotonin ; p-Chlorophenylalanine ; Immunohistochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The possibility that serotonin may influence the early response of astrocytes around a spinal cord trauma was investigated in a rat model by making a unilateral incision into the right dorsal horn of the T10-11 segments. One group of rats received a serotonin synthesis inhibitor, p-chlorophenylalanine (p-CPA) before injury in doses which cause a depletion of serotonin in the cord. Another group of traumatised rats did not receive p-CPA. All animals were allowed to survive for 5 h. Samples for immunohistochemistry were taken from the T9, T10-11 and T12 segments of the cord. Paraffin sections were immunostained for glial fibrillary acidic protein (GFAP) using monoclonal antibodies and avidin-biotin complex technique. Trauma to the cord resulted in a marked increase of GFAP immunoreactivity in all the investigated segments, particularly in the ipsilateral side. Pretreatment with p-CPA markedly reduced the GFAP response. This drug did not by itself influence the GFAP immunoreactivity of the cord of untraumatised rats. Our results show that trauma to the spinal cord induces a rapid enhancement of GFAP immunoreactivity in the cord which is present even far away from the primary lesion. This response can be prevented by pretreatment with the serotonin synthesis inhibitor, p-CPA. The results indicate that serotonin influences the increase of GFAP immunoreactivity following spinal cord injury either directly or indirectly, for instance by its microvascular reactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00228575
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Effect of cytoplasmic male-sterility in sorghum on host plant interaction with sorghum midge, Contarinia sorghicola (1993)
    Springer
    Euphytica 74 (1993), S. 35-39 
    Details
    ISSN: 1573-5060
    Keywords: Sorghum midge ; Contarinia sorghicola ; cytoplasmic male sterility ; host plant resistance ; resistance mechanisms ; sorghum ; Sorghum bicolor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Summary Sorghum midge, Contarinia sorghicola Coq. (Diptera: Cecidomyiidae) is one of the most important pests of grain sorghum worldwide. We studied the reaction of midge-resistant and midge-susceptible genic-cytoplasmic male-sterile (A-lines) and their maintainers (B-lines), and the effect of resistant and susceptible restorers on sorghum midge. Midge damage and adult emergence were significantly lower on the B-lines of midge-resistant genotypes (PM 7061 and PM 7068) than their corresponding A-lines, while the reverse was true for the midge-susceptible genotypes (296A and ICSA 42). Differences in midge damage and the number of midges emerged were not significant between the midge-resistant and midge-susceptible A-lines when infested without pollination (except midge emergence on PM 7061A). Pollination with a midge-resistant restorer (DJ6541) reduced midge emergence significantly in one of two seasons. Source of pollen did not influence midge emergence on the highly-resistant A-line, PM 7061A. The implications of these observations in the development of midge-resistant hybrids were discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00033764
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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